K-number	K233380
Device name	TRIDENT Mobile Fluoroscopy System
Applicant	Dornier Medtech America
Product code	JAA
Device class	Class II
Decision date	Jun 26, 2024
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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TRIDENT Mobile Fluoroscopy System

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